Detection of nucleic acids

Patent metadata

Field	Value
Publication number	US-10093967-B2
Application number	US-201514589467-A
Country	US
Kind code	B2
Filing date	Jan 5, 2015
Priority date	Aug 12, 2014
Publication date	Oct 9, 2018
Grant date	Oct 9, 2018

Abstract

Provided herein is technology relating to detecting and identifying nucleic acids and particularly, but not exclusively, to compositions, methods, kits, and systems for detecting, identifying, and quantifying target nucleic acids with high confidence at single-molecule resolution.

First claim

We claim:

1. A method for detecting a target nucleic acid in a sample, the method comprising:
a) immobilizing a single target nucleic acid molecule from the sample to a discrete region of a solid support and providing detectably labeled query probes that associate and dissociate with said single target nucleic acid according to a kinetic rate constant k on or k off that is greater than 1 min −1 ;
b) counting a plurality of time-resolved signal intensity transition events detected within the discrete region and identifying the signal intensity transition events as a candidate signal produced by the repeated association and dissociation of said detectably labeled query probes with said immobilized single target nucleic acid molecule when the number of signal intensity transition events detected within the discrete region is greater than a threshold value; and
c) detecting the target nucleic acid in the sample when said candidate signal is detected or when a value of a parameter characterizing said time-resolved signal intensity transition events indicates the presence of said single target nucleic acid molecule in said discrete region, wherein said parameter is selected from the group consisting of τ on , τ off , mean τ on , mean τ off , time-averaged τ on , time-averaged τ off , number of transitions, mean number of transitions, distribution of the number of transitions, mean of the distribution of the number of transitions, median of the distribution of the number of transitions, peak of the distribution of the number of transitions, standard deviation of the distribution of the number of transitions, and shape of the distribution of the number of transitions.

2. The method of claim 1 wherein the detectably labeled query probe is a nucleic acid or a fluorescent query probe.

3. The method of claim 1 wherein the discrete region of the solid support comprises a capture probe.

4. The method according to claim 1 wherein the parameter characterizing said time-resolved signal intensity transition events comprises one or more of;
i) a dwell time of the detectably labeled query probe in the discrete region of the solid support that is different than the dwell time of the detectably labeled query probe in the discrete region of the solid support in the absence of the target nucleic acid;
ii) a signal detected of the detectably labeled query probe in the discrete region of the solid support that is different than a signal detected of the detectably labeled query probe in the discrete region of the solid support in the absence of the target nucleic acid; or
iii) the number of signal intensity transition events detected within the discrete region is different than the number of signal intensity transition events detected within the discrete region in the absence of the target nucleic acid.

5. The method according to claim 1 wherein counting a plurality of time-resolved signal intensity transition events comprises observing the discrete region using a single-molecule resolution technique.

6. The method according to claim 1 wherein the detectably labeled query probe comprises a fluorescent label.

7. The method according to claim 1 wherein the target nucleic acid is a ribonucleic acid.

8. The method of claim 3 wherein the capture probe comprises a nucleic acid, a locked nucleic acid, a peptide nucleic acid, a nucleic acid binding protein, or an antibody.

9. The method of claim 1 further comprising producing a kinetic fingerprint from the time-resolved signal intensity transition events.

10. The method of claim 1 further comprising performing statistical treatment of the repeated binding of said detectably labeled query probes with said single target nucleic acid molecule.

11. The method of claim 1 wherein Poisson statistical treatment of said signal intensity transition events is used to discriminate target nucleic acids from non-target nucleic acids or said threshold value is calculated from hidden Markov modeling or an edge detection algorithm.

12. The method of claim 1 further comprising comparing said value of said parameter with a second value of said parameter calculated from a positive control nucleic acid, a negative control nucleic acid, or a second target nucleic acid comprising a different nucleotide sequence.

13. The method of claim 1 wherein the detectably labeled query probe consists of 5 to 15 nucleotides and the signal intensity transition events detected within the discrete region are recorded with a fluorescence detector.

14. A method of detecting a difference in a nucleotide sequence of a first nucleic acid relative to a second nucleic acid, the method comprising:
a) immobilizing a first single target nucleic acid molecule to a first discrete region of a solid support and immobilizing a second single target nucleic acid molecule to a second discrete region of said solid support, wherein the first target nucleic acid molecule comprises a first nucleotide sequence and the second target nucleic acid molecule comprises a second nucleotide sequence that is different than the first nucleotide sequence of the first target nucleic acid;
b) providing detectably labeled query probes that associate and dissociate with one or both single target nucleic acids according to a kinetic rate constant k on or k off that is greater than 1 min −1 ;
c) counting a plurality of time-resolved signal intensity transition events detected within said first discrete region and identifying the signal intensity transition events as a first candidate signal produced by the repeated association and dissociation of said detectably labeled query probes with said first single target nucleic acid molecule when the number of signal intensity transition events detected within the first discrete region is greater than a threshold value and counting a plurality of time-resolved signal intensity transition events detected within said second discrete region and identifying the signal intensity transition events as a second candidate signal produced by the repeated association and dissociation of said detectably labeled query probes with said second single target nucleic acid molecule when the number of signal intensity transition events detected, wherein said detectably labeled query probes all comprise the same known nucleotide sequence and the degree of complementarity between the detectably labeled query probes and the first target nucleic acid is different than the degree of complementarity between the detectably labeled query probes and the second target nucleic acid;
d) determining from the first candidate signal a first value of a parameter characterizing query probe association and dissociation with said first single target nucleic acid molecule and determining from the second candidate signal a second value of said parameter characterizing query probe association and dissociation with said second single target nucleic acid molecule; and
e) detecting a difference in the nucleotide sequence of the first nucleic acid relative to the second nucleic acid by comparing the first value of said parameter and the second value of said parameter, wherein a difference in the first and second values of said parameter indicates that the first and second target nucleic acids have different nucleotide sequences and wherein said parameter is selected from the group consisting of τon, τoff, mean τon, mean τoff, time-averaged τon, time-averaged τoff, number of transitions, mean number of transitions, distribution of the number of transitions, mean of the distribution of the number of transitions, median of the distribution of the number of transitions, peak of the distribution of

Assignees

• Univ Michigan Regents

Inventors

• Walter Nils
• Johnson-Buck Alexander
• Blanco Mario
• Rinaldi Arlie

Classifications

• C12Q1/6816

  characterised by the detection means (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6837 Primary

  using probe arrays or probe chips (C12Q1/6874 takes precedence) · CPC title

• C12Q1/6886

  for cancer (immunoassay for cancer G01N33/575) · CPC title

• C12Q2600/178

  miRNA, siRNA or ncRNA · CPC title

• C12Q2565/519

  characterised by the capture moiety being a single stranded oligonucleotide · CPC title